Syringomyelia Mimicking as Bibrachial Variant of Motor Neuron Disease.

Q3 Medicine
Tarun Ralot, Vinod Singh Jatav, Sameera Karimji, Vishwesh Sharma
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引用次数: 0

Abstract

Introduction: Syringomyelia is a slowly progressive degenerative disorder of the spinal cord. Clinical features of syringomyelia vary from weakness in limbs to positive sensory symptoms and dissociative sensory loss. Thus, early and prompt diagnosis becomes crucial for reducing the morbidity associated with the disease.

Case description: Here, we present a case of 52-year-old male presenting with progressive weakness in bilateral upper limbs without any sensory involvement which is an atypical presentation for syringomyelia.

Conclusion: Motor neuron disease (MND) like presentation in syringomyelia is a rare entity. This can make diagnosis of syringomyelia difficult. Hence, any patient presenting with pure motor weakness of bilateral upper limb should also be suspected of syringomyelia.

模拟脊髓空洞是运动神经元病的双臂变体。
脊髓空洞症是一种缓慢进行性脊髓退行性疾病。脊髓空洞症的临床特征从四肢无力到阳性感觉症状和分离性感觉丧失不等。因此,早期和及时的诊断对于减少与疾病相关的发病率至关重要。病例描述:在这里,我们报告一个52岁的男性病例,表现为双侧上肢进行性无力,没有任何感觉受累,这是脊髓空洞的不典型表现。结论:脊髓空洞的运动神经元病(MND)样表现是一种罕见的疾病。这使得脊髓空洞症的诊断变得困难。因此,任何表现为单纯双侧上肢运动无力的患者也应怀疑脊髓空洞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.80
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